Hanna MG - Search Results

1

MRPS25 mutations impair mitochondrial translation and cause encephalomyopathy.

Bugiardini E, Mitchell AL, Rosa ID, Horning-Do HT, Pitmann AM, Poole OV, Holton JL, Shah S, Woodward C, Hargreaves I, Quinlivan R, Amunts A, Wiesner RJ, Houlden H, Holt IJ, Hanna MG, Pitceathly RDS, Spinazzola A. Bugiardini E, et al. Among authors: hanna mg. Hum Mol Genet. 2019 Aug 15;28(16):2711-2719. doi: 10.1093/hmg/ddz093. Hum Mol Genet. 2019. PMID: 31039582 Free PMC article.

2

Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation.

Hanna MG, Nelson I, Sweeney MG, Cooper JM, Watkins PJ, Morgan-Hughes JA, Harding AE. Hanna MG, et al. Am J Hum Genet. 1995 May;56(5):1026-33. Am J Hum Genet. 1995. PMID: 7726155 Free PMC article.

3

Movement disorders and mitochondrial dysfunction.

Hanna MG, Bhatia KP. Hanna MG, et al. Curr Opin Neurol. 1997 Aug;10(4):351-6. doi: 10.1097/00019052-199708000-00012. Curr Opin Neurol. 1997. PMID: 9266161 Review.

4

Depletion of mitochondrial DNA by ddC in untransformed human cell lines.

Nelson I, Hanna MG, Wood NW, Harding AE. Nelson I, et al. Among authors: hanna mg. Somat Cell Mol Genet. 1997 Jul;23(4):287-90. doi: 10.1007/BF02674419. Somat Cell Mol Genet. 1997. PMID: 9542530

5

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

Hanna MG, Nelson IP, Rahman S, Lane RJ, Land J, Heales S, Cooper MJ, Schapira AH, Morgan-Hughes JA, Wood NW. Hanna MG, et al. Am J Hum Genet. 1998 Jul;63(1):29-36. doi: 10.1086/301910. Am J Hum Genet. 1998. PMID: 9634511 Free PMC article.

6

An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.

Clark KM, Taylor RW, Johnson MA, Chinnery PF, Chrzanowska-Lightowlers ZM, Andrews RM, Nelson IP, Wood NW, Lamont PJ, Hanna MG, Lightowlers RN, Turnbull DM. Clark KM, et al. Among authors: hanna mg. Am J Hum Genet. 1999 May;64(5):1330-9. doi: 10.1086/302361. Am J Hum Genet. 1999. PMID: 10205264 Free PMC article.

7

Genetics and molecular pathogenesis of mitochondrial respiratory chain diseases.

Hanna MG, Nelson IP. Hanna MG, et al. Cell Mol Life Sci. 1999 May;55(5):691-706. doi: 10.1007/s000180050327. Cell Mol Life Sci. 1999. PMID: 10379358 Review.

8

A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy.

Rahman S, Taanman JW, Cooper JM, Nelson I, Hargreaves I, Meunier B, Hanna MG, García JJ, Capaldi RA, Lake BD, Leonard JV, Schapira AH. Rahman S, et al. Among authors: hanna mg. Am J Hum Genet. 1999 Oct;65(4):1030-9. doi: 10.1086/302590. Am J Hum Genet. 1999. PMID: 10486321 Free PMC article.

9

Human mitochondrial DNA diseases.

Pulkes T, Hanna MG. Pulkes T, et al. Among authors: hanna mg. Adv Drug Deliv Rev. 2001 Jul 2;49(1-2):27-43. doi: 10.1016/s0169-409x(01)00124-7. Adv Drug Deliv Rev. 2001. PMID: 11377801 Review.

10

Human T cell leukaemia virus type I associated neuromuscular disease causing respiratory failure.

Littleton ET, Man WD, Holton JL, Landon DN, Hanna MG, Polkey MI, Taylor GP. Littleton ET, et al. Among authors: hanna mg. J Neurol Neurosurg Psychiatry. 2002 May;72(5):650-2. doi: 10.1136/jnnp.72.5.650. J Neurol Neurosurg Psychiatry. 2002. PMID: 11971056 Free PMC article.

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